<b><i>WT1 </i></b>Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome-Reference-Cited by-同舟云学术

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WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome

Published:2017 Issue:1 Volume:11 Page:34-39
ISSN:1661-5425
Container-title:Sexual Development
language:en
Short-container-title:Sex Dev

Author:

Guaragna Mara S.,Ribeiro de Andrade Juliana G.,de Freitas Carli Bárbara,Belangero Vera M.S.,Maciel-Guerra Andréa T.,Guerra-Júnior Gil,de Mello Maricilda P.

Publisher

S. Karger AG

Subject

Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Rare presentations of Wilms tumor in children: A case report;Iranian Journal of Pediatric Hematology & Oncology;2024-04-05

2. Wilms’ tumor gene 1: lessons from the interface between kidney development and cancer;American Journal of Physiology-Renal Physiology;2024-01-01

3. WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease;Sexual Development;2021-08-13

4. New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome;Medicine;2021-05-14

5. A novel WT1 gene mutation in a chinese girl with denys‐drash syndrome;Journal of Clinical Laboratory Analysis;2021-05

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